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Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes

✍ Scribed by Yves Sznajer; H. Annika Siitonen; Gaia Roversi; Chantal Dangoisse; Michèle Scaillon; France Ziereisen; Sylvie Tenoutasse; Marjo Kestilä; Lidia Larizza


Book ID
106121289
Publisher
Springer
Year
2007
Tongue
English
Weight
254 KB
Volume
167
Category
Article
ISSN
0340-6997

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